Variant report

Variant	nsv885902
Chromosome Location	chr6:54588069-54656673
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:307)
CpG islands
(count:0)
Chromatin interactive
region (count:47)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:54607728-54607745	K562	blood:	n/a	n/a
2	BATF	chr6:54596119-54596317	GM12878	blood:	n/a	n/a
3	CCNT2	chr6:54588403-54588563	K562	blood:	n/a	n/a
4	CEBPB	chr6:54602470-54602764	HepG2	liver:	n/a	chr6:54602618-54602629
5	CEBPB	chr6:54630892-54631129	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:54637537-54637832	HepG2	liver:	n/a	chr6:54637667-54637678 chr6:54637668-54637679 chr6:54637667-54637680
7	CEBPB	chr6:54613841-54614182	HepG2	liver:	n/a	chr6:54614009-54614020
8	CEBPB	chr6:54635080-54635165	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:54636911-54637077	HepG2	liver:	n/a	n/a
10	CTCF	chr6:54602167-54602363	GM13977	blood:	n/a	n/a
11	CTCF	chr6:54602120-54602270	NHEK	skin:	n/a	n/a
12	CTCF	chr6:54602105-54602358	Gliobla	brain:	n/a	n/a
13	CTCF	chr6:54622905-54622969	GM20000	blood:	n/a	n/a
14	CTCF	chr6:54602140-54602290	GM12868	blood:	n/a	n/a
15	CTCF	chr6:54602180-54602330	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr6:54602200-54602350	AG09309	skin:	n/a	n/a
17	CTCF	chr6:54602220-54602370	GM12867	blood:	n/a	n/a
18	CTCF	chr6:54601680-54601830	GM12874	blood:	n/a	n/a
19	CTCF	chr6:54602180-54602330	AG10803	skin:	n/a	n/a
20	CTCF	chr6:54602051-54602412	HepG2	liver:	n/a	n/a
21	CTCF	chr6:54602140-54602290	GM12872	blood:	n/a	n/a
22	CTCF	chr6:54602180-54602330	SAEC	small airway:	n/a	n/a
23	CTCF	chr6:54602219-54602284	MCF-7	breast:	n/a	n/a
24	CTCF	chr6:54602180-54602330	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr6:54602160-54602310	AG04450	lung:	n/a	n/a
26	CTCF	chr6:54602120-54602362	GM19238	blood:	n/a	n/a
27	CTCF	chr6:54602177-54602318	GM13976	blood:	n/a	n/a
28	CTCF	chr6:54602200-54602350	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr6:54602160-54602310	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr6:54602180-54602330	HL-60	blood:	n/a	n/a
31	CTCF	chr6:54602160-54602310	HEK293	kidney:	n/a	n/a
32	CTCF	chr6:54602160-54602310	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr6:54602040-54602190	WI-38	lung:	n/a	n/a
34	CTCF	chr6:54602180-54602330	GM12866	blood:	n/a	n/a
35	CTCF	chr6:54602180-54602330	NB4	blood:	n/a	n/a
36	CTCF	chr6:54602240-54602390	GM12872	blood:	n/a	n/a
37	CTCF	chr6:54602120-54602344	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:54602156-54602332	A549	lung:	n/a	n/a
39	CTCF	chr6:54602100-54602250	WI-38	lung:	n/a	n/a
40	CTCF	chr6:54602220-54602370	GM12864	blood:	n/a	n/a
41	CTCF	chr6:54602165-54602339	LNCaP	prostate:	n/a	n/a
42	CTCF	chr6:54602140-54602290	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr6:54602160-54602310	K562	blood:	n/a	n/a
44	CTCF	chr6:54602125-54602369	GM12878	blood:	n/a	n/a
45	CTCF	chr6:54602134-54602329	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:54602220-54602370	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr6:54602220-54602370	GM12875	blood:	n/a	n/a
48	CTCF	chr6:54602180-54602330	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr6:54602220-54602370	RPTEC	kidney:	n/a	n/a
50	CTCF	chr6:54602180-54602330	GM12873	blood:	n/a	n/a

No data

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:54600974..54603157-chr6:54603359..54605565,2	MCF-7	breast:
2	chr6:54594502..54597427-chr6:54632424..54633945,2	MCF-7	breast:
3	chr6:54588605..54590894-chr6:54594243..54596836,3	MCF-7	breast:
4	chr6:54620515..54622977-chr6:54710478..54712259,2	MCF-7	breast:
5	chr6:54577593..54590845-chr6:54708062..54715554,67	MCF-7	breast:
6	chr6:54589684..54593022-chr6:54593846..54596999,3	MCF-7	breast:
7	chr6:54615642..54618179-chr6:54622767..54625294,2	MCF-7	breast:
8	chr6:54585837..54588493-chr6:54594744..54597239,2	MCF-7	breast:
9	chr6:54633061..54636995-chr6:54710354..54713223,5	MCF-7	breast:
10	chr6:54611159..54612903-chr6:54616738..54619073,2	MCF-7	breast:
11	chr6:54596975..54599172-chr6:54626479..54629322,2	MCF-7	breast:
12	chr6:54580831..54596896-chr6:54704751..54716103,89	MCF-7	breast:
13	chr6:54644390..54646954-chr6:54709633..54712699,3	MCF-7	breast:
14	chr6:54621367..54623899-chr6:54711418..54713643,2	MCF-7	breast:
15	chr6:54641381..54644333-chr6:54709873..54712755,2	MCF-7	breast:
16	chr6:54615642..54618179-chr6:54622767..54625294,2	MCF-7	breast:
17	chr6:54596752..54599206-chr6:54723703..54726514,2	MCF-7	breast:
18	chr6:54594616..54597518-chr6:54631395..54633965,2	MCF-7	breast:
19	chr6:54591002..54596706-chr6:54709941..54714732,14	MCF-7	breast:
20	chr6:54597254..54599876-chr6:54711300..54712858,2	MCF-7	breast:
21	chr6:54611159..54612903-chr6:54616738..54619073,2	MCF-7	breast:
22	chr6:54562310..54563986-chr6:54587468..54589771,2	MCF-7	breast:
23	chr6:54594502..54597427-chr6:54632424..54633945,2	MCF-7	breast:
24	chr6:54561293..54570100-chr6:54582505..54590247,14	MCF-7	breast:
25	chr6:54600974..54603157-chr6:54603359..54605565,2	MCF-7	breast:
26	chr6:54588428..54589294-chr6:54730022..54730672,2	MCF-7	breast:
27	chr6:54581587..54585941-chr6:54586924..54591451,7	MCF-7	breast:
28	chr6:54573340..54575837-chr6:54587895..54589989,2	MCF-7	breast:
29	chr6:54625827..54630691-chr6:54708545..54714193,7	MCF-7	breast:
30	chr6:54588605..54590894-chr6:54594243..54596836,3	MCF-7	breast:
31	chr6:54648395..54650437-chr6:54710257..54713518,3	MCF-7	breast:
32	chr6:54586807..54589626-chr6:54590506..54593407,2	MCF-7	breast:
33	chr6:54564726..54568882-chr6:54587061..54590275,4	MCF-7	breast:
34	chr6:54627133..54632625-chr6:54707387..54713886,8	MCF-7	breast:
35	chr6:54596908..54599664-chr6:54710614..54713357,2	MCF-7	breast:
36	chr6:54594451..54596147-chr6:54739921..54742591,2	MCF-7	breast:
37	chr6:54640508..54643660-chr6:54711207..54713141,3	MCF-7	breast:
38	chr6:54589684..54593022-chr6:54593846..54596999,3	MCF-7	breast:
39	chr6:54589905..54593836-chr6:54739903..54743144,4	MCF-7	breast:
40	chr6:54585837..54588493-chr6:54594744..54597239,2	MCF-7	breast:
41	chr6:54600004..54603656-chr6:54710742..54713977,4	MCF-7	breast:
42	chr6:54596975..54599172-chr6:54626479..54629322,2	MCF-7	breast:
43	chr6:54585158..54588149-chr6:54741239..54743201,2	MCF-7	breast:
44	chr6:54594616..54597518-chr6:54631395..54633965,2	MCF-7	breast:
45	chr6:54587916..54591176-chr6:54736715..54740306,4	MCF-7	breast:
46	chr6:54586807..54589626-chr6:54590506..54593407,2	MCF-7	breast:
47	chr6:54586929..54589873-chr6:54742420..54744071,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM83B-3	chr6:54635608-54636037	NONHSAT113225
2	lnc-FAM83B-3	chr6:54635169-54635601	NONHSAT113225

No data

Variant related genes	Relation type
KRASP1	TF binding region
RNU6-1023P	TF binding region
ENSG00000224984	chromatin interactions
ENSG00000168143	chromatin interactions

Extended variants
information (count: 2406 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2406 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6459021	chr6:54588069-54588070	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558302377	chr6:54588085-54588086	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs550143269	chr6:54588092-54588093	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs142317395	chr6:54588173-54588174	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558642804	chr6:54588192-54588193	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs183404431	chr6:54588218-54588219	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs537878933	chr6:54588283-54588284	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554937893	chr6:54588291-54588292	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs561833539	chr6:54588334-54588335	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs375046187	chr6:54588336-54588337	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs574702056	chr6:54588348-54588349	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs12661765	chr6:54588362-54588363	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs76027153	chr6:54588363-54588364	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs554142544	chr6:54588373-54588374	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577526475	chr6:54588428-54588429	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546401157	chr6:54588470-54588471	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs974798	chr6:54588498-54588499	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs186612966	chr6:54588526-54588527	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs191518080	chr6:54588607-54588608	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs114348085	chr6:54588609-54588610	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs561736414	chr6:54588675-54588676	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs184036690	chr6:54588693-54588694	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs547694512	chr6:54588695-54588696	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs570380143	chr6:54588728-54588729	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188396798	chr6:54588733-54588734	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs536617697	chr6:54588758-54588759	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs115227880	chr6:54588826-54588827	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192857423	chr6:54588889-54588890	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537957215	chr6:54588941-54588942	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs75779064	chr6:54588947-54588948	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs568462103	chr6:54588951-54588952	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185472133	chr6:54589034-54589035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs16885901	chr6:54589037-54589038	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs554480731	chr6:54589053-54589054	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556550427	chr6:54589098-54589099	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs531307706	chr6:54589142-54589143	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs59960057	chr6:54589191-54589192	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs182218436	chr6:54589247-54589248	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs556783724	chr6:54589312-54589313	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs372676412	chr6:54589358-54589359	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs576670337	chr6:54589367-54589368	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs571352278	chr6:54589370-54589371	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs1507106	chr6:54589376-54589377	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs574292765	chr6:54589379-54589380	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs375710615	chr6:54589419-54589420	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs115916426	chr6:54589443-54589444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs34077285	chr6:54589488-54589489	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs561602372	chr6:54589522-54589523	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs370335584	chr6:54589529-54589530	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs1507107	chr6:54589539-54589540	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54583600-54594200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr6:54587200-54594200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:54587400-54594200	Weak transcription	NHEK	skin
4	chr6:54594200-54594400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:54594200-54594800	Enhancers	NHEK	skin
6	chr6:54594200-54595000	Enhancers	HMEC	breast
7	chr6:54594200-54595200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr6:54594200-54595600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:54594400-54595000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:54594400-54595600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:54594600-54595600	Enhancers	Fetal Intestine Small	intestine
12	chr6:54594800-54595000	Flanking Active TSS	NHEK	skin
13	chr6:54594800-54595400	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr6:54595000-54595200	Flanking Active TSS	HMEC	breast
15	chr6:54595000-54595200	Enhancers	NHEK	skin
16	chr6:54595000-54595600	Enhancers	Duodenum Mucosa	Duodenum
17	chr6:54595000-54595800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:54595200-54595400	Flanking Active TSS	NHEK	skin
19	chr6:54595200-54595600	Enhancers	Brain Substantia Nigra	brain
20	chr6:54595200-54595600	Enhancers	Fetal Intestine Large	intestine
21	chr6:54595200-54595600	Enhancers	HMEC	breast
22	chr6:54595400-54595800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr6:54595400-54595800	Enhancers	NHEK	skin
24	chr6:54595600-54599800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:54595800-54596200	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr6:54599800-54600200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:54600200-54612400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:54601400-54613800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr6:54612400-54612600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:54612600-54613200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr6:54612600-54613400	Enhancers	NHEK	skin
32	chr6:54613000-54613400	Enhancers	HMEC	breast
33	chr6:54613200-54613400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr6:54614000-54614200	Enhancers	Liver	Liver
35	chr6:54622200-54623400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:54622800-54623600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:54622800-54623600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr6:54622800-54623800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr6:54623000-54623600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr6:54623000-54623800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr6:54623000-54624000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr6:54623200-54623600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:54623200-54623600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:54623400-54624000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr6:54628200-54628800	Enhancers	Brain Substantia Nigra	brain
46	chr6:54637000-54640400	Weak transcription	Fetal Heart	heart
47	chr6:54640000-54640800	Enhancers	Fetal Lung	lung
48	chr6:54640400-54641000	Enhancers	Fetal Heart	heart
49	chr6:54641200-54641400	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr6:54641400-54642200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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